Chondrogenic differentiation of human mesenchymal stem cells: a comparison between micromass and pellet culture systems

Chondrogenic differentiation of human mesenchymal stem cells: a comparison between micromass and pellet culture systems
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人间充质干细胞的软骨分化:微团和颗粒培养系统之间的比较

DOI:
10.1007/s10529-010-0293-x
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发表时间:
2010-09-01
影响因子:
2.7
通讯作者:
Huang, Dongsheng
Huang, Dongsheng
中科院分区:
工程技术4区
文献类型:
--
作者:
Zhang, Liangming;Su, Peiqiang;Huang, Dongsheng

文献摘要

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高密度细胞培养是人骨髓间充质干细胞向软骨细胞分化的关键。两种高密度细胞培养系统,微团和沉淀培养,已被用来诱导hMSCs的软骨分化。在微团培养中,诱导软骨组织更大,更均匀,富含软骨特异性胶原蛋白II,但纤维软骨样特征,胶原蛋白I和肥大软骨细胞特征,胶原蛋白X,显着减少相比,那些在小球培养。真实的RT-PCR结果显示,微团培养中II型胶原和聚集蛋白聚糖mRNA表达上调,而X型胶原和I型胶原mRNA表达下调。因此,微团培养系统是体外软骨形成研究的一个有前途的工具。
High-density cell culture is pivotal for the chondrogenic differentiation of human mesenchymal stem cells (hMSCs). Two high-density cell culture systems, micromass and pellet culture, have been used to induce chondrogenic differentiation of hMSCs. In micromass culture, the induced-cartilage tissues were larger, more homogenous and enriched in cartilage-specific collagen II but the fibrocartilage-like feature, collagen I, and hypertrophic chondrocyte feature, collagen X, were markedly decreased compared to those in pellet culture. Furthermore, real time RT-PCR analysis demonstrated that collagen II and aggrecan mRNA were up-regulated while collagen X and collagen I mRNA were down-regulated in micromass culture. Thus, the micromass culture system is a promising tool for in vitro chondrogenic studies.